Forest types of the Wapiti, Doon and Glaisnock catchments, ranked in order of proportion of preferred food species for deer, paralleled a gradient of landform stability. Seral forests and low altitude silver beech forests were preferred deer habitat because they contained the largest proportions of highly preferred species. They often occurred on unstable landforms such as debris cones, colluvi...

1 In forest communities, species coexistence can be favoured by disturbance-related variations in light regime coupled with rank reversal in species performance. The objective of this study was to determine if a major canopy disturbance, resulting from an ice storm, would favour the coexistence of sugar maple ( Acer saccharum ) and beech ( Fagus grandifolia ) in an old-growth forest located nea...

Anticipated changes in climate and research findings on the drought sensitivity of beech have triggered controversial discussions about the future of European beech. We investigated the growth response of beech on the treeand stand-level in mature stands to three different thinning intensities (no thinning, strong thinning, very strong thinning) on a northeastand southwest-facing slope in South...

Specialist herbivores are thought to often enhance or maintain plant diversity within ecosystems, because they prevent their host species from becoming competitively dominant. In contrast, specialist herbivores are not generally expected to have negative impacts on non-hosts. However, we describe a cascade of indirect interactions whereby a specialist sooty mold (Scorias spongiosa) colonizes th...

European beech (Fagus sylvatica L., hereafter beech), one of the major native tree species in Europe, is known to be drought sensitive. Thus, the identification of critical thresholds of drought impact intensity and duration are of high interest for assessing the adaptive potential of European beech to climate change in its native range. In a common garden experiment with one-year-old seedlings...

During the last meeting in Karlsruhe the authors presented a paper [1] providing background information about the determination of the characteristic bending strength of beech glulam. A design proposal was derived to calculate the characteristic bending strength depending on the characteristic tensile strength of the lamellae and the characteristic finger joint bending strength. It was experime...

Global change—particularly climate change, forest management, and atmospheric deposition—has significantly altered forest growing conditions in Europe. The influences of these changes on beech growth (Fagus sylvatica L.) were investigated for the past 80 years in Belgium, using non-linear mixed effects models on ring-width chronologies of 149 mature and dominant beech trees (87–186 years old). ...

Northern hardwoods have undergone a marked change in their dynamics, with American beech (Fagus grandifolia Ehrh.) increasing in abundance relative to sugar maple (Acer saccharum Marsh.). This study aims to better understand this sudden shift in recruitment dynamics. We performed an extensive analysis of the age structure, radial growth pattern, and release history on >700 saplings from 34 matu...

Following a full mast production in autumn 1995 in the old growth beech forest of la Tillaie, France, cupules, live and dead yearling seedlings were counted in September 1996 in 40 plots, embracing a wide range of ecological conditions. The influence of geomorphology and forest stage on mast production and on seedling establishment and survival was studied. Maximum seedling abundance did not oc...

Norway spruce (Picea abies) forests exhibit lower annual atmospheric methane consumption rates than do European beech (Fagus sylvatica) forests. In the current study, pmoA (encoding a subunit of membrane-bound CH(4) monooxygenase) genes from three temperate forest ecosystems with both beech and spruce stands were analyzed to assess the potential effect of tree species on methanotrophic communit...